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FDA 510(k)

TN-RD-50

K-Number: K932598 · 1994-06-03

ApplicantKeithley Instruments, Inc.
Decision Date1994-06-03
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TN-RD-50 is the device name listed in this FDA 510(k) record. The listed applicant is Keithley Instruments, Inc.. It received FDA 510(k) clearance on 1994-06-03 under 510(k) number K932598. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TN-RD-50?

TN-RD-50 is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Keithley Instruments, Inc.. The 510(k) number is K932598.

When did TN-RD-50 receive FDA 510(k) clearance?

TN-RD-50 received FDA 510(k) clearance on 1994-06-03, under 510(k) number K932598.

Who is the listed applicant for TN-RD-50?

The FDA 510(k) record lists Keithley Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TN-RD-50?

The FDA product code for TN-RD-50 is IYE.

Other records listing Keithley Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K942083ADVANCED THERAPY DOSIMETERK874893MODEL 35300 TRACKER(TM) THERAPY BEAM EVALUATORK854110KEITHLEY MODEL 75100 & 75200

Related Devices (Code: IYE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261865AerFrame™ Alignment Laser Box (LBV2)Stabilix, LLCK261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA Radiation Therapy Information System (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser Applikationen

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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